Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10049390
rs10049390
10 0.776 0.080 3 133982275 intron variant G/A snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs1011970
rs1011970
22 0.677 0.320 9 22062135 intron variant G/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs10152518
rs10152518
9 0.790 0.080 15 67884824 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1028166
rs1028166
9 0.790 0.080 4 181892145 intron variant G/A snv 0.74 0.700 1.000 1 2014 2014
dbSNP: rs1035209
rs1035209
9 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 0.700 1.000 2 2014 2019
dbSNP: rs10411210
rs10411210
13 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
dbSNP: rs10457678
rs10457678
10 0.790 0.080 6 138801103 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs10505477
rs10505477
31 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
dbSNP: rs10506868
rs10506868
16 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs10511330
rs10511330
10 0.776 0.080 3 114402172 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs1057517558
rs1057517558
APC
3 0.882 0.120 5 112839549 frameshift variant C/- delins 0.700 0
dbSNP: rs1057941
rs1057941
18 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs10774214
rs10774214
9 0.790 0.080 12 4259186 intron variant T/C snv 0.54 0.700 1.000 4 2013 2019
dbSNP: rs1078643
rs1078643
10 0.776 0.080 17 10803924 missense variant G/A;C snv 0.700 1.000 3 2019 2019
dbSNP: rs10795668
rs10795668
17 0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 0.700 1.000 4 2008 2019
dbSNP: rs10821907
rs10821907
12 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs10849432
rs10849432
9 0.790 0.080 12 6276561 intergenic variant C/T snv 0.84 0.700 1.000 2 2014 2016
dbSNP: rs10849433
rs10849433
10 0.776 0.080 12 6297738 regulatory region variant T/C snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs10849438
rs10849438
9 0.790 0.080 12 6302870 intergenic variant T/G snv 1.0E-01 0.700 1.000 1 2019 2019
dbSNP: rs10904849
rs10904849
9 0.790 0.080 10 16955267 intron variant G/A;T snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs10911251
rs10911251
9 0.790 0.080 1 183112059 intron variant A/C snv 0.37 0.700 1.000 2 2013 2019
dbSNP: rs10936599
rs10936599
32 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 0.700 1.000 1 2010 2010
dbSNP: rs10951878
rs10951878
9 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10980628
rs10980628
10 0.776 0.080 9 110909123 intron variant T/C snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs11064437
rs11064437
9 0.790 0.080 12 6872998 splice acceptor variant C/T snv 9.3E-02 0.700 1.000 1 2016 2016